Mutations reference genome

Hi all!

Are you planning to align the mutations data to the reference genome hg38 (GRCh38) instead of hg19? I know that since a while you aligned RNA expression, fusions and copy number data to hg38, but variants are still called by using hg19 as far as I know.



Hi Pedro!

We updated our mutation calling pipeline as of 22Q4, and our mutation data will be aligned to hg38 from now on. Stay tuned for the 22Q4 release!